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510(k) Premarket Notification Database

Device Classification Name:	TAPE, TELEVISION & VIDEO, ENDOSCOPIC
Regulation Number:	876.1500 [See Other Products with this regulation number]
510(k) Number:	K032545
Device Name:	ENDOSCOPIC LIGHT SOURCE LS-3000X; LS-1800XG/MED LIGHT X 180; LS-2500H/MED LIGHT H 250
Applicant:	MGB ENDOSKOPISCHE GERATE GMBH (BERLIN) SCHWARZSCHILDSTRASSE 6 BERLIN,
Contact:	JOHANNES TSCHEPE
Product Code:	FET [See Other Manufacturers that make this Product]
Date Received:	08-18-2003
Decision Date:	09-02-2003
Decision:	SE
Advisory Committee:	GU
Statement/Summary/Purged Status:	Summary
Type:	Traditional
Review by Third Party:	Y
Expedited Review:	N

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